Modelling failure mechanisms to explain rock slope change along the Isle of Purbeck coast,UK

Results are presented of distinct element computer modelling used to examine rates and mechanisms of change in rock slopes and cliffs, where material intact properties determine process and form but the most significant controls are the joint pattern and cross-joint properties. The modelling approach does not appear to have been used before in a geomorphological context and provides an alternative approach for examining cliff development. Field and laboratory data have been collected for the Portland Limestone outcrop of the Isle of Purbeck, central southern England. The Portland Limestome is a hard, shelly, crystalline sediment of the Upper Jurassic. It has a regular discontinuity pattern throughout the outcrop in Purbeck. While joint orientation remains relatively constant, bedding changes from horizontal to vertical, a consequence of the Purbeck Monocline. There are resulting implications for spatial variations in rock slope evolution. The modelling exercise enhances previous knowledge on rock failure mechanisms and slope development along the Purbeck coast and demonstrates its potential in research where landforms are developed in lithified, jointed rock masses. © 1998 John Wiley & Sons, Ltd.     

热扩散驱动的元素分异和同位素分馏:一种不容忽视的硅酸盐成分分异机制

热扩散在地质过程中是否发挥重要作用一直存有争议。本文回顾了热扩散的研究历史和现状,重点总结了热扩散驱动的元素和同位素行为规律,并探讨了温度、硅酸盐组分、压力和氧逸度等因素对热扩散行为的影响。已有的研究表明,稳定热梯度下的硅酸盐热扩散效应类似于结晶分异或AFC过程,可以造成轻、重同位素分别在高温端和低温端富集,而主、微量元素的扩散方向则取决于两端化学势的高低和熔体中的电价平衡。从基性岩浆到酸性岩浆,熔体聚合度增大,黏度增加,热扩散速率明显降低,成网元素的热扩散效应减弱,变网元素则反之;水、氟、氯和硫化氢等挥发组分能增加熔体的非桥氧比例,降低熔体聚合度,因而能显著增强硅酸盐熔体中元素和同位素的热扩散效应。在此基础上,本文提出了当前硅酸盐体系热扩散研究中存在的五个亟需解决的问题,即:1)对不同硅酸盐体系的热扩散规律的研究还不够全面;2)对微量元素的热扩散行为认识不足;3)硅酸盐体系热扩散作用的影响因素及尺度还不够明确;4)热扩散作用的地质与地球化学关键识别标志有待确立;5)硅酸盐体系热扩散作用的理论模型有待建立。尽管硅酸盐体系热扩散的研究还存在诸多不足,但越来越多的证据表明,热扩散是地质过程中不容忽视的一种成分分异机制。这种机制会造成岩浆房或岩浆通道中的元素分异和同位素分馏,可能对于一些成分分异的岩石和矿床的形成具有重要的意义。     

SH波地表散射的局域边界元模拟

本文提出了一种计算不规则起伏地形中SH波散射的有效方法——局域边界元法.本方法基于传统边界元法,为计算复杂地表散射问题提供了一种更加高效的解决方案.根据地震波满足的边界积分方程中牵引力格林函数的特性,我们将自由边界分解成水平部分和起伏部分.通过公式推导,可将水平部分的位移由起伏部分的位移通过格林函数线性叠加表示,因此只需对起伏部分的位移进行直接求解,从而极大地减少了待求解的未知数个数,显著提高了计算效率.通过与半圆形山谷SH波平面波入射的解析解比较,验证了方法的正确性.数值模型比较显示,局域边界元模拟结果与传统边界元数值解完全吻合,但是大幅提高了计算效率.因此,局域边界元法可以作为模拟不规则地形中地震波散射的有效工具.     

汶川地震震前龙门山以西地壳垂直隆升机理分析

结合流动GPS观测速度场及层析成像结果,构建跨龙门山断裂剖面的二维有限元分层模型,分两种情况讨论汶川地震前龙门山前缘地壳垂直隆升的物理机制,以及中、下地壳软物质垂向和横向的不均匀性对地壳隆升作用的影响。分析认为：川西高原相对四川盆地的差异抬升和龙门山以西地壳缩短的共同作用是汶川地震震前龙门山前缘地壳垂直隆升的可能原因。     

山脊线与坡度和峰值速度放大系数的相关性研究

地形效应是地震工程和地震学的重要研究内容.数值方法是研究地形效应的重要工具.然而以往关于地形特征对地形效应的影响的研究大多是基于二维简单模型.对三维真实地形特征和地震动放大的关系缺乏详细的研究.为了更好地描述三维地形特征,本文将地形用不同的地形特征因子来描述,并用算法将它们从地形数据中提取出来.从而使地形和放大系数的相关性的研究转换为不同地形特征因子和放大系数的相关性的研究上.本文中,我们选择芦山地区作为研究对象,用算法提取出特征因子山脊线和坡度.它们分别表征了山脊形态和山体的陡峭程度.我们又用谱元法分别模拟三种不同主频Ricker子波的地震波在起伏地表和水平地表模型中的传播,并得到了它们各自的峰值速度(PGV)放大系数.通过分析三个主频的PGV放大系数在山脊线上分布,我们发现放大系数幅值在山脊线上分布不均匀.放大系数较高的地方位于山脊线弯曲或宽度发生变化的附近.我们又统计了三个放大系数在滑动平均坡度上分布,并得到了放大系数均值和坡度的正相关曲线.结果表明坡度和放大系数两者在幅值分布上具有正相关性.     

论韧性剪切带研究及其地质意义

系统研究韧性剪切带变形岩在天然强剪切应力作用条件下常量元素迁移机制及活化转移的应力排序、微量元素迁移的动力控制、稀土元素配分变化和变形矿物晶体化学变异的应力制约等构成了当代韧性剪切带研究的前沿课题,也是当前糜棱岩岩石地球化学研究难点和精华所在。其研究成果将对动力成岩（成矿）机理的认识有重要的突破,具有重要的理论意义和潜在应用价值。对韧性剪切带及其变形岩石的研究现状和研究意义进行系统的综述,提出了未来韧性剪切带及其糜棱岩的研究方向和目标: ①系统研究糜棱岩中主要造岩矿物组合及其变形特征,计算剪切变形岩石的应力—应变参数,搞清韧性剪切带所处的应力应变环境;②系统研究韧性剪切带岩石在天然分强剪切应力作用条件下常量元素迁移机制及活化转移的应力排序问题;③系统研究剪切变形作用过程中岩石化学组成的微量和稀土元素变化,讨论强变形条件下岩石中微量元素活化和迁移规律,深入探讨微量元素迁移的动力控制,包括稀土元素配分变化的应力制约以及应变矿物晶格化学变化行为及其对其寄主的变形岩石元素（组分）在应变过程中迁移变化的制约和影响;④从理论上探讨天然强剪切应变条件下岩石中组分活化、转移与应力（应变）的因果联系,为深入探讨韧性剪切带动力成岩（成矿）作用提供理论的科学依据,为探讨中、下地壳中韧性剪切带的形成和演化提供科学依据（如韧性剪切带金的富集）,同时为韧性剪切变形作用条件下成岩、成矿地球化学作用提供理论和实验依据;⑤现代分析技术如激光同位素原位分析以及激光ICP MASS分析技术对研究变形域内的岩石（矿物）的元素和同位素的活化迁移规律,对深刻揭示糜棱岩化过程中的元素活化迁移机制提供更高质量的地球化学证据具有重要的作用。     

不同节点布置下二维涡激振动的无单元法参数化分析

尝试建立1种基于无单元法的涡激振动数值模拟算法,并给出适用于涡激振动分析的前处理自动布点方法.基于无单元法理论,使用动最小二乘法构造形函数,利用无单元伽辽金法,采用速度和压力分离模式,及手工布点和自动布点2种方法所得出的节点布置形式,对流场控制方程进行空间离散,模拟二维涡激振动的流场形态,并对VIV相关参数进行分析,计算不同节点布置情况下的升力系数(Cl)、曳力系数(Cd)及斯特罗哈数(St),并与物理模型实验结果进行对比.计算结果表明,无单元伽辽金法应用于立管VIV分析是可行的,且文中采用2种布点方法均能较好的模拟流场中泻涡脱落的形态,计算结果与传统方法和物理模型实验结果吻合良好.证明文中2种布点方法都能用于固定圆柱的二维VIV分析,但自动布点法能够更好地适用于复杂问题的计算及圆柱体在流场中的VIV动力响应分析.     

Arctic freshwater ostracods from modern periglacial environments in the Lena River Delta (Siberian Arctic,Russia): geochemical applications for palaeoenvironmental reconstructions

The aim of this study is to describe ostracods from freshwater habitats in the Siberian Arctic in order to estimate the present-day relationships between the environmental setting and the geochemical properties of ostracod calcite. A special focus is on the element ratios (Mg/Ca, Sr/Ca), and the stable isotope composition (δ¹⁸O, δ¹³C), in both ambient waters and ostracod calcite. The most common species are Fabaeformiscandona pedata and F. harmsworthi with the highest frequency in all studied waters. Average partition coefficients D(Sr) of F. pedata are 0.33 ± 0.06 (1σ) in females, and 0.32 ± 0.06 (1σ) in males. A near 1:1 relationship of δ¹⁸O was found, with a mean shift of Δ_mean = 2.2‰ ± 0.5 (1σ) to heavier values in ostracod calcite of F. pedata as compared to ambient waters. The shift is not dependent on δ¹⁸O_water, and is caused by metabolic (vital) and temperature effects. Temperature-dependence is reflected in the variations of this shift. For ostracod calcite of F. pedata a vital effect as compared to inorganic calcite in equilibrium was quantified with 1.4‰. Results of this study are valuable for the palaeoenvironmental interpretation of geochemical data of fossil ostracods from permafrost deposits.     

Transformation from Permian to Quaternary bauxite in southwestern South China Block driven by superimposed orogeny: A case study from Sanhe ore deposit

Permian karstic bauxite and its Quaternary derivative, in western Guangxi, southwestern, South China Block, possess a total tonnage greater than 0.5 billion tons. The primary late Permian karstic bauxite formed in reduced environment in the background of Tethyan accretionary orogenesis. And as one consequence of Cenozoic convergence of the Indian and Eurasia continents, the primary orebody was uplifted, eroded and re-sedimented within Quaternary laterite. The geochemical variation and its controls during the ore transformation from Permian to Quaternary remain poorly understood. Quaternary ore blocks comprise an inner zone of fresh ore, and then it gradually transited through a middle zone to a margin with extensive weathering. One such bauxite block was selected and further subdivided into twenty-three samples for geochemical and mineralogical analysis. The inner and middle zones contain similar mineralogical compositions, dominated by diaspore and amesite, with minor illite, anatase, goethite, pyrite, zircon, and rutile. The margin is composed of diaspore, with small amounts of amesite, boehmite, illite, goethite, anatase, kaolinite, zircon, rutile, and barite. Bauxite in all three zones is composed of mainly Al, Si, Fe, and Ti, and high contents of Zr, Cr, Li, F, S, Zn, V, Sr, Nb, Ba, and REE. Variations in Fe²⁺ and Fe³⁺ between the three zones were observed. The elements Si, Al, Fe²⁺, Mg, Ba, Cr, F, Li, Ni, Zn, and REE decrease from the core of the ore block outwards, corresponding to an increase in S and Fe³⁺. Depletions in Si, Al, Fe²⁺, Mg, Ba, and Cr were caused by the dissolution of amesite. Most of the Al and Si in amesite were lost during the weathering, and minor retained to form kaolinite. Depletions in Li, Ni, and Zn resulted from changes in the depositional environment between the late Permian and Quaternary. Dissolution of REE-bearing fluorocarbonates resulted in depletions of REE and F. The enrichment of Fe³⁺ and S was related to the precipitation of goethite, hematite, and barite in an oxidizing environment, while local enrichment of Ce resulted from the redox change of Ce³⁺ → Ce⁴⁺ under the same condition. This shows that the chemical composition of laterite enwrapping the bauxite also took part in Quaternary bauxite transformation. This study shows that the elements migrations during bauxite transformation were influenced by multiple independent factors except for the elemental attributes.     

Determination of microscopic parameters of quartz sand through tri-axial test using the discrete element method

A calibration procedure, in which coupled effects of microscopic parameters are considered, is proposed to determine the values of the microscopic parameters in the Discrete Element Method (DEM) for Fujian quartz sand. Laboratory tri-axial tests are conducted to be compared with the DEM simulations and the effects of end restraint in the laboratory tests are eliminated through a digital image measurement system. Sensitivities of the macroscopic behaviour of the specimen to the microscopic parameters are analyzed through DEM simulations. Four coupled effects of the microscopic parameters on the macroscopic behaviour are investigated through a graphic method and then considered in the calibration procedure.